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American Osteopathic Association’s research marks Vitamin D inefficiency owing to Low…
The Journal of the American Osteopathic Association signified inefficiency of Vitamin D that can't be metabolized owing to low Magnesium Levels that implies Vitamin D remains stored and…
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Merck asserts the ANMAT’S approval for MAVENCLAD tablets for treating multiple sclerosis
Leading Science and technology company, Merck announced that the Argentinian Administration of Medicines, Food and Medical Technology has sanctioned the registration of MAVENCLAD …
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Lantern Pharma joins Genomic England’s Discovery Forum industry partnership
Genomics England and Lantern Pharma that emphasizes on precision oncology incorporating Artificial intelligence asserted that Lantern will associate with Genomics England's Discovery…
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Amgen sought CHMP’s positive opinion on XGEVA for multiple myeloma
Amgen asserted that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted a positive opinion to expand the current indication for…
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Jazz enrolls First Patient in Phase 2 Clinical Trial evaluating Defibrotide
Jazz Pharmaceuticals asserted the enrollment of patients in a Phase 2 Clinical Trial evaluating the efficacy and safety of defibrotide for the prevention of acute…
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Stephen Ostroff, Deputy Commissioner for FVMNTP states draft report on Bisphenol A
Stephen Ostroff, M.D., Deputy Commissioner for Foods and Veterinary Medicine on National Toxicology Program draft report on Bisphenol A stating that "We base our regulatory decisions on…
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Aurinia appoints Michael Hayden to its Board of Directors
Aurinia Pharmaceuticals which is a clinical stage bio pharmaceutical company aiming to enhance its global immunology market appointed Michael Hayden,CM OBC MB ChB PhD FRCP (C) FRSC to…
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Pfizer appointed Albert Bourla to its Board of Directors
Pfizer claimed the appointment of Albert Bourla, DVM,Ph.D to its Board off Directors with effect from immediately.
Dr.Albert Bourla is currently the Chief operating officer of…
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MabSpace Biosciences declares FDA approval of IND for MSB2311
MabSpace Biosciences declares FDA cleared investigational New Drug for MSB2311 which is a humanized programmed death protein-ligand 1 (PD-L1) antibody for the treatment of patients with…
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Kadmon declares updated optimistic results of Phase 2 study of KD025-208 in cGVHD
Kadmon Holdings claimed positive results from ongoing Phase 2 Clinical trial KD025-208 assessing updated optimistic results from an ongoing Phase 2 Clinical Trial KD025-208 evaluating…
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Puma Biotechnology asserts CHMP’s negative opinion on MAA for Neratinib
Puma Biotechnology asserted that the Committee for Medicinal Products for Human Use of the European Medicines Agency has adopted a negative opinion thereby refuting to grant Marketing…
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NaviGate Cardiac Structures declares GATE bioprosthesis to treat tricuspid regurgitation
NaviGate Cardiac Structures asserted that its catheter-guided GATE valved-stent bioprosthesis became the first Canadian orthotopic valve replacement to treat severe tricuspid…
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Clovis Oncology sought positive vote from CHMP for Rucaparib tablets
Clovis Oncology claimed an update to the ongoing regulatory review for the Marketing Authorization Application (MAA) for Rucaparib tablets as monotherapy for the treatment of advanced…
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Celgene affirmed Antitrust Clearance for obtaining Juno
Celgene Corporation asserted that the applicable waiting period under the Hart-Scott-Rodino Antitrust Improvements Act of 1976 ("HSR") with respect to the previously announced tender…
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Biologics assures availability of ERLEADA treatment for Non-Metastatic, Castration-Resistant…
McKesson Specialty Health oncology and complex care pharmacy services company has been finalized by the Janssen Pharmaceutical Companies of Johnson & Johnson which is considered the…
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Vertex commences Phase 3 Study of VX-659 for CF
Vertex Pharmaceuticals affirmed initiating the first Phase 3 study of VX-659, tezacaftor and ivacaftor as an investigational triple combination regimen for people with cystic fibrosis…
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FDA monitors destruction and recall of kratom products
U.S FDA had asserted the destruction and recall of large volume of kratom-containing dietary supplements that is ideally manufactured and distributed nationwide under the Brand names…
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Dr. Warren Krackov appointed Medical Director and UFE Specialist for Vascular Interventions
Dr. Warren Krackov, interventional radiologist specializing in minimally invasive treatment for dialysis access management and other vascular conditions has been named medical director…
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Alabama Fertility offers INVOcell in Alabama
Medical device company, INVO Bioscience sought FDA clearance for Intravaginal Culture System, INVOcell asserted that Alabama Fertility has augmented its scope of reproductive treatments…
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Evofem Biosciences sought FDA’s Fast Track designation for Amphora vagina gel
Biotechnology company developing innovative products to fill women's unmet healthcare needs, Evofem Biosciences asserted that the U.S FDA has extended Fast Track designation for Amphora…
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